Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Andrea M. Gortva"'
Publikováno v:
Journal of the American Chemical Society. 116:5150-5154
Fluoride ion induced generation of isobutylidene from isopropyl trimethylsilyl ketone enol triflate in the presence of 6,6-dimethylfulvene gives the [2.2]-m-cyclophane dimer of [alpha],[alpha],[alpha][prime],[alpha][prime]-tetramethyl-m-xylylene. Whe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::213960c7b90ffa2ae5d8e5df55aba005
https://doi.org/10.1021/ja00091a018
https://doi.org/10.1021/ja00091a018
Publikováno v:
ChemInform. 25
Fluoride ion induced generation of isobutylidene from isopropyl trimethylsilyl ketone enol triflate in the presence of 6,6-dimethylfulvene gives the [2.2]-m-cyclophane dimer of [alpha],[alpha],[alpha][prime],[alpha][prime]-tetramethyl-m-xylylene. Whe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac6e4f6da34f35ad53d923c17fc4c209
https://doi.org/10.1002/chin.199446068
https://doi.org/10.1002/chin.199446068
Autor:
Joseph J. Gajewski, Andrea M. Gortva
Publikováno v:
The Journal of Organic Chemistry. 54:373-378
3-Methylene-1,4-cyclohexadiene, 1,5-methylene-1,3-cyclohexadiene, 2, 1-methylene-1,4-dihydronaphthalene, 5, and 9-methylene-9,10-dihydroanthracene, 8, react with second-order kinetics in benzene solution. The activation parameters for the reaction of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8922b8f2f018ef378cf3a228871fdd3
https://doi.org/10.1021/jo00263a021
https://doi.org/10.1021/jo00263a021
Publikováno v:
Chemischer Informationsdienst. 17
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b56feeadd272cf1bfddc51cb2f0cf556
https://doi.org/10.1002/chin.198626108
https://doi.org/10.1002/chin.198626108
Autor:
Joseph J. Gajewski, Andrea M. Gortva
Publikováno v:
ChemInform. 20
3-Methylene-1,4-cyclohexadiene, 1,5-methylene-1,3-cyclohexadiene, 2, 1-methylene-1,4-dihydronaphthalene, 5, and 9-methylene-9,10-dihydroanthracene, 8, react with second-order kinetics in benzene solution. The activation parameters for the reaction of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c228d5d0e5897a85b7bb6368f26f44c
https://doi.org/10.1002/chin.198933067
https://doi.org/10.1002/chin.198933067
Publikováno v:
Journal of the American Chemical Society. 108:1083-1084
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80d562b6d28c5960203a108a68170c72
https://doi.org/10.1021/ja00265a040
https://doi.org/10.1021/ja00265a040
Autor:
Andrea M. Gortva, Joseph J. Gajewski
Publikováno v:
Journal of the American Chemical Society. 104:334-335
Despite intensive study of the pyrolysis of C/sub 7/H/sub 8/ compounds, the methylenecyclohexadienes, o- and p-isotoluenes, 1 and 2, respectively, have received little attention. Both 1 and 2 are ca. 23 kcal/mol less stable than toluene, and so their
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb7e072605d6a755b16b44851783ba09
https://doi.org/10.1021/ja00365a081
https://doi.org/10.1021/ja00365a081